A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269633



Internal ID20836673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83113759..83115262hg38UCSC Ensembl
chr5:82409578..82411081hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg381504
hg191504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565064
Supporting Variants
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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